Secondary findings from whole-exome sequencing data in families with familial combined hyperlipidemia (FCHL)
Abstract Background During the interpretation of genome sequencing data, some types of secondary findings are identified that are located in genes that do not appear to be related to the causes of the primary disease. Although these are not the primary targets for evaluation, they have a high risk f...
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Autores principales: | , , , , , , |
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Formato: | article |
Lenguaje: | EN |
Publicado: |
SpringerOpen
2021
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Materias: | |
Acceso en línea: | https://doaj.org/article/afaf98bd8d0e48ea855a03ff061ae77b |
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